Evidence map›Paper›PMID 26263500›Full record

ArticleeLife2015

The viral context instructs the redundancy of costimulatory pathways in driving CD8(+) T cell expansion.

Suzanne P M Welten, Anke Redeker, Kees L M C Franken, Jennifer D Oduro, Ferry Ossendorp, Luka Čičin-Šain, Cornelis J M Melief, Peter Aichele, Ramon Arens

Open access · goldAbstract read
In one paragraph

Article in eLife, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.0field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

43 citing papers in PubMed, 58 citations in OpenAlex.

  1. Article
  2. CD8 T Cell Sensing of Type I Interferon Impacts Anergy.European journal of immunology · 2026
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  10. The lncRNAeLife · 2023
    Article
  11. Delayed vaccine-induced CD8Journal for immunotherapy of cancer · 2023
    Article
  12. Article
  13. Article
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  15. Article
  16. Article
  17. Article
  18. Combination blockade of OX40L and CD30L inhibits allergen-driven memory TThe Journal of allergy and clinical immunology · 2021
    Article
  19. Article
  20. The curious case of IL-33 in homeostasis and infection.European journal of immunology · 2021
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 2 countries.

Suzanne P M WeltenDepartment of Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, Netherlands.
Anke RedekerDepartment of Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, Netherlands.
Kees L M C FrankenDepartment of Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, Netherlands.
Jennifer D OduroDepartment for Vaccinology/Immune Aging and Chronic Infection, Helmholtz-Zentrum für Infektionsforschung GmbH, Braunschweig, Germany.
Ferry OssendorpDepartment of Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, Netherlands.
Luka Čičin-ŠainDepartment for Vaccinology/Immune Aging and Chronic Infection, Helmholtz-Zentrum für Infektionsforschung GmbH, Braunschweig, Germany.
Cornelis J M MeliefDepartment of Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, Netherlands.
Peter AicheleDepartment of Medical Microbiology and Hygiene, Institute of Immunology, University of Freiburg, Freiburg, Germany.
Ramon ArensDepartment of Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, Netherlands.
Leiden University Medical Center · NLHelmholtz Centre for Infection Research · DEInstitute of Medical Microbiology and Hygiene · DEMedizinische Hochschule Hannover · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Signals delivered by costimulatory molecules are implicated in driving T cell expansion. The requirements for these signals, however, vary from dispensable to essential in different infections. We examined the underlying mechanisms of this differential T cell costimulation dependence and found that the viral context determined the dependence on CD28/B7-mediated costimulation for expansion of naive and memory CD8(+) T cells, indicating that the requirement for costimulatory signals is not imprinted. Notably, related to the high-level costimulatory molecule expression induced by lymphocytic choriomeningitis virus (LCMV), CD28/B7-mediated costimulation was dispensable for accumulation of LCMV-specific CD8(+) T cells because of redundancy with the costimulatory pathways induced by TNF receptor family members (i.e., CD27, OX40, and 4-1BB). Type I IFN signaling in viral-specific CD8(+) T cells is slightly redundant with costimulatory signals. These results highlight that pathogen-specific conditions differentially and uniquely dictate the utilization of costimulatory pathways allowing shaping of effector and memory antigen-specific CD8(+) T cell responses.

Indexed as

AnimalsCD8-Positive T-LymphocytesIntercellular Signaling Peptides and ProteinsLymphocytic choriomeningitis virusMice, Inbred C57BLMuromegalovirusIntercellular Signaling Peptides and Proteinscostimulationimmunologyinfectious diseasemicrobiologymouseT cellsviral infection

Identifiers

PMID26263500
PMCPMC4558566
OpenAlexW2199601526

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.